Variant report

Variant	esv1794667
Chromosome Location	chr12:1174917-1199813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:1179144-1179336	K562	blood:	n/a	n/a
2	ATF2	chr12:1189964-1190438	GM12878	blood:	n/a	n/a
3	ATF2	chr12:1189942-1190432	GM12878	blood:	n/a	n/a
4	BACH1	chr12:1192252-1192568	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr12:1189802-1190073	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:1189805-1190045	GM12878	blood:	n/a	n/a
7	BCL3	chr12:1189974-1190400	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:1193133-1193153	GM12878	blood:	n/a	n/a
9	BRCA1	chr12:1189702-1189919	GM12878	blood:	n/a	n/a
10	CEBPB	chr12:1175921-1176099	A549	lung:	n/a	n/a
11	CEBPB	chr12:1179104-1179418	IMR90	lung:	n/a	chr12:1179365-1179378 chr12:1179365-1179376
12	CEBPB	chr12:1175887-1176058	IMR90	lung:	n/a	n/a
13	CEBPB	chr12:1175918-1176030	K562	blood:	n/a	n/a
14	CHD2	chr12:1189680-1189927	GM12878	blood:	n/a	n/a
15	CHD2	chr12:1189730-1189921	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr12:1189980-1190374	GM12878	blood:	n/a	n/a
17	CREB1	chr12:1189981-1190471	GM12878	blood:	n/a	n/a
18	CTCF	chr12:1175520-1175670	AG09319	gingival:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
19	CTCF	chr12:1175540-1175690	AG04449	skin:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
20	CTCF	chr12:1175560-1175710	GM12866	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
21	CTCF	chr12:1175560-1175710	HepG2	liver:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
22	CTCF	chr12:1175560-1175710	HEEpiC	esophagus:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
23	CTCF	chr12:1175580-1175730	GM12867	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
24	CTCF	chr12:1175506-1175719	K562	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
25	CTCF	chr12:1175560-1175710	GM12868	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
26	CTCF	chr12:1175520-1175670	GM12870	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
27	CTCF	chr12:1175523-1175733	LNCaP	prostate:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
28	CTCF	chr12:1175560-1175710	GM12875	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
29	CTCF	chr12:1175466-1175721	IMR90	lung:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
30	CTCF	chr12:1175500-1175650	NHDF-neo	bronchial:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
31	CTCF	chr12:1175543-1175682	GM20000	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
32	CTCF	chr12:1175495-1175727	GM13977	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
33	CTCF	chr12:1175580-1175730	HCM	heart:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
34	CTCF	chr12:1175560-1175710	AG09309	skin:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
35	CTCF	chr12:1175542-1175686	ProgFib	skin:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
36	CTCF	chr12:1175507-1175721	LNCaP	prostate:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
37	CTCF	chr12:1175560-1175710	Hela-S3	cervix:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
38	CTCF	chr12:1175560-1175710	GM12878	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
39	CTCF	chr12:1175560-1175710	GM12864	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
40	CTCF	chr12:1175560-1175710	HMF	breast:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
41	CTCF	chr12:1175560-1175710	HRE	kidney:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
42	CTCF	chr12:1175500-1175650	HCM	heart:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
43	CTCF	chr12:1175517-1175715	HUVEC	blood vessel:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
44	CTCF	chr12:1175460-1175610	HAc	cerebellar:	n/a	n/a
45	CTCF	chr12:1175459-1175751	A549	lung:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
46	CTCF	chr12:1175544-1175682	Pancreas_OC	pancreas:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
47	CTCF	chr12:1175542-1175703	Hela-S3	cervix:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
48	CTCF	chr12:1175415-1175800	GM12878	blood:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
49	CTCF	chr12:1175536-1175678	SK-N-SH_RA	brain:	n/a	chr12:1175606-1175624 chr12:1175607-1175623
50	CTCF	chr12:1175500-1175650	Hela-S3	cervix:	n/a	chr12:1175606-1175624 chr12:1175607-1175623

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1192425-1192475	HAEpiC	amniotic membrane:	n/a
2	chr12:1192425-1192475	SK-N-SH_RA	brain:	n/a
3	chr12:1192425-1192475	GM12878	blood:	n/a
4	chr12:1192425-1192475	Caco-2	colon:	n/a
5	chr12:1192425-1192475	SK-N-SH	brain:	n/a
6	chr12:1192425-1192475	HepG2	liver:	n/a
7	chr12:1192425-1192475	SKMC	muscle:	n/a
8	chr12:1192425-1192475	GM06990	blood:	n/a
9	chr12:1192425-1192475	NH-A	brain:	n/a
10	chr12:1192425-1192475	IMR90	lung:	fetal
11	chr12:1192425-1192475	BE2_C	brain:	n/a
12	chr12:1192425-1192475	ProgFib	skin:	n/a
13	chr12:1192425-1192475	HCF	heart:	n/a
14	chr12:1192425-1192475	HEK293	kidney:	embryo
15	chr12:1192425-1192475	HUVEC	blood vessel:	n/a
16	chr12:1192425-1192475	HCPEpiC	choroid plexus:	n/a
17	chr12:1192425-1192475	PFSK-1	brain:	n/a
18	chr12:1192425-1192475	A549	lung:	n/a
19	chr12:1192425-1192475	Jurkat	blood:	n/a
20	chr12:1192425-1192475	NB4	blood:	n/a
21	chr12:1192425-1192475	AoSMC	blood vessel:	n/a
22	chr12:1192425-1192475	AG09319	gingival:	n/a
23	chr12:1192425-1192475	HEEpiC	esophagus:	n/a
24	chr12:1192425-1192475	HL-60	blood:	n/a
25	chr12:1192425-1192475	HRCEpiC	kidney:	n/a
26	chr12:1192425-1192475	NHDF-neo	bronchial:	n/a
27	chr12:1192425-1192475	T-47D	breast:	n/a
28	chr12:1192425-1192475	AG10803	skin:	n/a
29	chr12:1192425-1192475	PrEC	prostate:	n/a
30	chr12:1192425-1192475	HMEC	breast:	n/a
31	chr12:1192425-1192475	HIPEpiC	eye:	n/a
32	chr12:1192425-1192475	NT2-D1	testis:	n/a
33	chr12:1192425-1192475	U87	brain:	n/a
34	chr12:1192425-1192475	CMK	blood:	n/a
35	chr12:1192425-1192475	GM19239	blood:	n/a
36	chr12:1192425-1192475	HCM	heart:	n/a
37	chr12:1192425-1192475	HCT-116	colon:	n/a
38	chr12:1192425-1192475	H1-hESC	embryonic stem cell:	embryo
39	chr12:1192425-1192475	AG04450	lung:	fetal
40	chr12:1192425-1192475	HRE	kidney:	n/a
41	chr12:1192425-1192475	ECC-1	luminal epithelium:	n/a
42	chr12:1192425-1192475	AG09309	skin:	n/a
43	chr12:1192425-1192475	HNPCEpiC	eye:	n/a
44	chr12:1192425-1192475	LNCaP	prostate:	n/a
45	chr12:1192425-1192475	BJ	skin:	n/a
46	chr12:1192425-1192475	RPTEC	kidney:	n/a
47	chr12:1192425-1192475	ovcar-3	ovarian:	n/a
48	chr12:1192425-1192475	GM12891	blood:	n/a
49	chr12:1192425-1192475	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:1192425-1192475	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1057331..1059748-chr12:1192287..1193829,2	MCF-7	breast:
2	chr12:1175408..1176101-chr12:1202225..1202957,2	MCF-7	breast:
3	chr12:1106383..1108991-chr12:1173040..1176603,3	MCF-7	breast:
4	chr12:1099164..1100750-chr12:1199458..1202097,2	MCF-7	breast:
5	chr12:1099907..1102555-chr12:1186671..1189258,2	K562	blood:

Variant related genes	Relation type
ERC1	TF binding region
ERC1	CpG island
ENSG00000082805	chromatin interactions
ENSG00000002016	chromatin interactions
ENSG00000250132	chromatin interactions

Extended variants
information (count: 886 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1859451	chr12:1174917-1174918	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559742039	chr12:1174964-1174965	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530005380	chr12:1174974-1174975	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs80171416	chr12:1174975-1174976	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189056338	chr12:1174976-1174977	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573234750	chr12:1174982-1174983	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147985101	chr12:1174986-1174987	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181553226	chr12:1174997-1174998	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570654272	chr12:1175097-1175098	Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534956754	chr12:1175104-1175105	Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115450438	chr12:1175125-1175126	Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186518780	chr12:1175128-1175129	Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566802182	chr12:1175192-1175193	Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557036845	chr12:1175213-1175214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191459581	chr12:1175252-1175253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141612697	chr12:1175267-1175268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146393932	chr12:1175346-1175347	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181102889	chr12:1175363-1175364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544529500	chr12:1175411-1175412	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs541722623	chr12:1175441-1175442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186176336	chr12:1175442-1175443	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs553759047	chr12:1175463-1175464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs549273659	chr12:1175485-1175486	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574790095	chr12:1175487-1175488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561629384	chr12:1175492-1175493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs541889596	chr12:1175657-1175658	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138457696	chr12:1175659-1175660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs34999895	chr12:1175724-1175725	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs568735345	chr12:1175741-1175742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537604559	chr12:1175748-1175749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528226242	chr12:1175771-1175772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs59619170	chr12:1175819-1175820	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs568232254	chr12:1175832-1175833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571245565	chr12:1175833-1175834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146122744	chr12:1175843-1175844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568510328	chr12:1175856-1175857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139808562	chr12:1175857-1175858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189719495	chr12:1175875-1175876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs149794665	chr12:1175886-1175887	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs534879229	chr12:1175904-1175905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376195258	chr12:1175921-1175922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs541524156	chr12:1175925-1175926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs144714573	chr12:1175959-1175960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs74709510	chr12:1176002-1176003	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs386375371	chr12:1176003-1176004	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs35134824	chr12:1176020-1176021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11830345	chr12:1176042-1176043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs557428540	chr12:1176066-1176067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183517238	chr12:1176133-1176134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546323161	chr12:1176148-1176149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Autism	22495311	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1153400-1200400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:1163800-1200200	Weak transcription	Ovary	ovary
3	chr12:1169000-1183400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:1169800-1175200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
5	chr12:1170000-1192600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr12:1172800-1176400	Weak transcription	Thymus	Thymus
7	chr12:1173400-1175000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr12:1173400-1177200	Weak transcription	Liver	Liver
9	chr12:1173800-1176600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:1173800-1180000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:1173800-1182400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr12:1173800-1192400	Weak transcription	Primary T cells from cord blood	blood
13	chr12:1174000-1176600	Weak transcription	Colon Smooth Muscle	Colon
14	chr12:1174000-1176600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr12:1174000-1179200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr12:1174000-1179200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:1174000-1183400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr12:1174000-1186000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:1174000-1186400	Weak transcription	Fetal Lung	lung
20	chr12:1174000-1190400	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr12:1174000-1196200	Weak transcription	Primary B cells from cord blood	blood
22	chr12:1174200-1176200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:1174200-1183400	Weak transcription	Fetal Stomach	stomach
24	chr12:1174200-1201600	Weak transcription	A549	lung
25	chr12:1174400-1177200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:1175000-1175200	Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr12:1175200-1192600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:1175200-1211600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr12:1176600-1176800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:1176600-1176800	Enhancers	Colon Smooth Muscle	Colon
31	chr12:1176600-1177000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr12:1176600-1177000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:1176600-1177000	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr12:1176800-1192000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:1177000-1177800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr12:1177000-1180000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:1177800-1178400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr12:1178400-1178800	Enhancers	Fetal Heart	heart
39	chr12:1178400-1179400	Enhancers	HUVEC	blood vessel
40	chr12:1178400-1184000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr12:1178400-1187200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr12:1178600-1186600	Weak transcription	NHDF-Ad	bronchial
43	chr12:1178800-1186400	Weak transcription	Fetal Heart	heart
44	chr12:1179200-1179400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:1179200-1179400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr12:1179200-1179800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr12:1179400-1186400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:1179400-1189800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr12:1179400-1193400	Weak transcription	HUVEC	blood vessel
50	chr12:1179600-1179800	Enhancers	Lung	lung

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